Clinical Research Coordinator A/B ( Department of Medicine - Renal Division)
Company: University of Pennsylvania
Location: Philadelphia
Posted on: April 25, 2025
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Job Description:
University Overview The University of Pennsylvania, the largest
private employer in Philadelphia, is a world-renowned leader in
education, research, and innovation. This historic, Ivy League
school consistently ranks among the top 10 universities in the
annual U.S. News & World Report survey. Penn has 12 highly-regarded
schools that provide opportunities for undergraduate, graduate and
continuing education, all influenced by Penn's distinctive
interdisciplinary approach to scholarship and learning. As an
employer Penn has been ranked nationally on many occasions with the
most recent award from Forbes who named Penn one of America's Best
Large Employers in 2023. Penn offers a unique working environment
within the city of Philadelphia. The University is situated on a
beautiful urban campus, with easy access to a range of educational,
cultural, and recreational activities. With its historical
significance and landmarks, lively cultural offerings, and wide
variety of atmospheres, Philadelphia is the perfect place to call
home for work and play. The University offers a competitive
benefits package that includes excellent healthcare and tuition
benefits for employees and their families, generous retirement
benefits, a wide variety of professional development opportunities,
supportive work and family benefits, a wealth of health and
wellness programs and resources, and much more. Posted Job Title
Clinical Research Coordinator A/B ( Department of Medicine - Renal
Division) Job Profile Title Clinical Research Coordinator A Job
Description Summary Job Description Job Responsibilities
Coordinator A: This position will assist in the management of
multiple clinical trials and responsibilities in specific research
area. Coordinate the screening of patients, subject enrollment,
collection and storage of biological samples and related study
documents, and collection of clinical data. Assist with
Institutional Review Board (IRB) filings and inquiries, and assist
in the preparation of manuscripts, grant proposals, and research
related presentations. Works closely with the Principal
Investigator, manager, and study team to identify problems and
develop solutions. Implement approved changes to procedures as
needed and monitor results. Responsible for study coordination for
investigator-initiated studies, multi-center research studies, and
patient-oriented clinical and translational research projects.
* Coordinate and conduct clinical studies, includes; subject
recruitment, informed consent, chart maintenance and data entry
* Coordinate IRB submissions and renewals in accordance with FDA
and IRB guidelines
* Assure compliance with the protocol and regulatory requirements
includes: collecting, recording, and maintaining data and source
documentations.
* Oversee study preparation and blood sample processing and
analysis
* Database management and analysis
* Ordering and stocking supplies, maintaining equipment
* Educate patients and family members
* Promote good clinical practice in the conduct of clinical
investigations, included possessing an in-depth knowledge of the
federal regulations and guidance documents for the conduct of
clinical studies and human subject protection
* Other duties and responsibilities as assigned Coordinator B:
Participate in and coordinate clinical trials within the Penn
Department of Medicine's Clinical Trials Unit. The person will
support a diverse group of investigators, involving work on a wide
spectrum of clinical trials ranging from phase I to IV,
investigator and industry initiated, different disease states and
varying complexities. Involvement in trials will range from
consulting to serving as the primary coordinator for a study
handling all coordinator activities such as:
Assist in development of study documents. Communicate with study
team members and regulatory review boards. Recruit, consent and
screen patients according to protocol. Schedule patient visits and
any necessary testing. Conduct patient visits. Monitor patients per
protocol requirements and ensure adherence to protocol
requirements. Organize and maintain all documentation required by
the Investigator, sponsor or CRO, includes source documentation,
case report forms, and research charts. Collect, review and report
study data. Complete case report forms and resolve data queries.
Process and ship study specimens including blood and urine.
Participate in initiation, monitoring, audit and close-out visits.
Participate in study team meetings, and ongoing protocol training.
Assist in the development/maintenance of study specific case report
forms and source document tools. Show vigilance in patient safety,
protocol compliance and data qualify. Adhere to all University of
Pennsylvania, FDA and GCP guidelines. CONTINGENT UPON FUNDING
Qualifications Effective problem solving abilities; effective
communication and writing skills; strong organizational and time
management skills; flexible and able to multi-task; demonstrated
ability to work as part of a team, as well as independently;
knowledge of IRB and human research protection regulations; prior
experience in gene therapy trials preferred Coordinator A: Bachelor
of Science and 1 to 2 years of experience or equivalent combination
of education and experience is required. Coordinator B: Bachelor of
Science and 2 to 4 years of experience or equivalent combination of
education and experience is required. Job Location - City, State
Philadelphia, Pennsylvania Department / School Perelman School of
Medicine Pay Range $46,500.00 - $52,661.00 Annual Rate Salary
offers are made based on the candidate's qualifications,
experience, skills, and education as they directly relate to the
requirements of the position, and in alignment with salary ranges
based on external market data for the job's level. Internal
organization and peer data at Penn are also considered. Equal
Opportunity Statement The University of Pennsylvania is an equal
opportunity employer. Candidates are considered for employment
without regard to race, color, sex, sexual orientation, religion,
creed, national origin (including shared ancestry or ethnic
characteristics), citizenship status, age, disability, veteran
status or any class protected under applicable federal, state or
local law. Special Requirements
Background checks may be required after a conditional job offer is
made. Consideration of the background check will be tailored to the
requirements of the job. University Benefits
Keywords: University of Pennsylvania, Lakewood , Clinical Research Coordinator A/B ( Department of Medicine - Renal Division), Healthcare , Philadelphia, New Jersey
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